BESST + Standard Care for Suicide Prevention
Trial Summary
What is the purpose of this trial?
The goal of this pilot randomized controlled trial is to test an adapted suicide prevention program (the Building VA Engagement, Self-efficacy, and Social Support To Prevent Suicide or BESST) in rural Veterans discharged from community care mental health treatment settings. The main question it aims to answer is: * Does BESST combined with standard care improve suicide-related outcomes among this population compared to standard care alone? Participants will be assigned by change to a treatment group. Some will receive the BESST intervention combined with standard care, and some will receive standard care alone. All participants will be in this research study for up to three months. Those receiving the BESST intervention will have: * 1 one-hour brief educational session; * Seven follow-up check-ins (\~30 minutes each) All participants will have three assessment interviews where they will be asked about their mental health and treatment received outside of the VA. The investigators will compare participants assigned to the BESST intervention combined with standard care vs participants assigned to standard care alone to see if the BESST intervention improves suicide-related outcomes.
Do I have to stop taking my current medications for this trial?
The trial protocol does not specify whether you need to stop taking your current medications. It seems likely that you can continue them, but you should confirm with the study team.
Do I need to stop my current medications to join the trial?
The trial information does not specify whether you need to stop taking your current medications. It is best to discuss this with the study team or your healthcare provider.
What data supports the idea that BESST + Standard Care for Suicide Prevention is an effective treatment?
The available research does not provide specific data on BESST + Standard Care for Suicide Prevention. However, it does highlight the effectiveness of other treatments for suicide prevention. For example, a study on a multidisciplinary aftercare program showed significant improvements in resilience, well-being, and reduced suicidal thoughts. Another study on a group intervention for veterans found that integrating skills training and social support with safety planning could benefit those at high risk for suicide. These findings suggest that comprehensive and supportive approaches can be effective in reducing suicidal behavior.12345
What data supports the effectiveness of the treatment BESST for suicide prevention?
Research shows that programs combining social support and skills training, like BESST, can improve self-efficacy (confidence in one's ability to manage situations) and reduce suicidal thoughts. A study on a similar approach found significant improvements in resilience, well-being, and reduced distress among participants.12345
What safety data exists for BESST + Standard Care for Suicide Prevention?
The provided research does not directly mention safety data for BESST or Building VA Engagement, Self-efficacy, and Social Support To Prevent Suicide. The studies focus on other interventions like SAFER and SAFE VET, which are related to suicide prevention among veterans but do not provide specific safety data for BESST.36789
Is the treatment BESST a promising treatment for suicide prevention?
Yes, BESST is a promising treatment for suicide prevention because it focuses on building engagement, self-efficacy, and social support, which are important factors in reducing suicidal thoughts and behaviors. The approach aligns with successful strategies like providing support and care after a suicide attempt, which have shown to improve resilience and well-being.27101112
How is the BESST treatment different from other suicide prevention treatments?
Research Team
Natalie Riblet, MD MPH
Principal Investigator
White River Junction VA Medical Center
Eligibility Criteria
This trial is for Veterans over 18, recently discharged from VA community mental health care, at risk of self-harm, and connected to specific VAMCs. They must speak English and be able to consent. Those not clinically appropriate or in vulnerable groups won't be included.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive the BESST intervention combined with standard care or standard care alone
Follow-up
Participants are monitored for safety and effectiveness after treatment
Treatment Details
Interventions
- BESST
Find a Clinic Near You
Who Is Running the Clinical Trial?
White River Junction Veterans Affairs Medical Center
Lead Sponsor
VHA Office of Rural Health
Collaborator